|
OMIM |
Link |
Information gain |
01 |
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.00111569
|
|
|
LSA
|
[NCBI]
|
0.000631402
|
|
|
DFSP
|
[NCBI]
|
0.000343073
|
|
|
DDD
|
[NCBI]
|
0.000330618
|
|
|
gorlin-chaudhry-moss syndrome
|
[NCBI]
|
0.000176746
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
0.000151553
|
|
|
amyloidosis, primary cutaneous
|
[NCBI]
|
0.000131131
|
|
|
EGFR
|
[NCBI]
|
6.65863e-05
|
|
|
SHOC2
|
[NCBI]
|
6.5181e-05
|
|
|
CBX5
|
[NCBI]
|
5.58153e-05
|
|
|
SLC35D2
|
[NCBI]
|
5.14307e-05
|
|
|
LHX3
|
[NCBI]
|
3.87339e-05
|
|
|
EGF
|
[NCBI]
|
3.86144e-05
|
|
|
CBL
|
[NCBI]
|
3.73816e-05
|
|
|
RB1
|
[NCBI]
|
2.15393e-05
|
|
|
MBP
|
[NCBI]
|
1.75923e-05
|
|
|
RNASE3
|
[NCBI]
|
1.03918e-05
|
|
|
CEACAM5
|
[NCBI]
|
5.25447e-06
|
|
|
AR
|
[NCBI]
|
4.64542e-06
|
|
|
PCNA
|
[NCBI]
|
3.46126e-06
|
|